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13-HODE, 9-HODE and ALOX15 as potential players in Rett syndrome OxInflammation.
- Source :
-
Free radical biology & medicine [Free Radic Biol Med] 2019 Apr; Vol. 134, pp. 598-603. Date of Electronic Publication: 2019 Feb 08. - Publication Year :
- 2019
-
Abstract
- Mutations in the MECP2 gene are the main cause of Rett syndrome (RTT), a pervasive neurodevelopmental disorder, that shows also multisystem disturbances associated with a metabolic component. The aim of this study was to investigate whether an increased production of oxidized linoleic acid metabolites, specifically 9- and 13-hydroxyoctadecadienoic acids (HODEs), can contribute to the altered the redox and immune homeostasis, suggested to be involved in RTT. Serum levels of 9- and 13-HODEs were elevated in RTT and associated with the expression of arachidonate 15-Lipoxygenase (ALOX15) in peripheral blood mononuclear cells (PBMCs). Omega-3 polyunsaturated fatty acids supplementation has shown to lower HODEs levels in RTT. Statistically significant correlation was demonstrated between the increased plasma HODEs levels and the lipoprotein-associated phospholipase A2 (Lp-PLA2) activity. Collectively, these findings reinforce the concept of the key role played by lipid peroxidation in RTT, and the possible ability of omega-3 polyunsaturated fatty acids supplementation in improving the oxinflammation status in RTT.<br /> (Copyright © 2019. Published by Elsevier Inc.)
- Subjects :
- Adolescent
Adult
Arachidonate 15-Lipoxygenase genetics
Case-Control Studies
Child
Female
Humans
Inflammation genetics
Inflammation metabolism
Leukocytes, Mononuclear metabolism
Male
Rett Syndrome genetics
Rett Syndrome metabolism
Young Adult
Arachidonate 15-Lipoxygenase metabolism
Inflammation pathology
Linoleic Acids metabolism
Linoleic Acids, Conjugated metabolism
Rett Syndrome pathology
Subjects
Details
- Language :
- English
- ISSN :
- 1873-4596
- Volume :
- 134
- Database :
- MEDLINE
- Journal :
- Free radical biology & medicine
- Publication Type :
- Academic Journal
- Accession number :
- 30743046
- Full Text :
- https://doi.org/10.1016/j.freeradbiomed.2019.02.007